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Discovery of Potent Allosteric DRP1 Inhibitors by Disrupting Protein-Protein Interaction with MiD49.

Takeru FuruyaJean LinArina AfanasevaLisa MolzBharat LaguBin Ma
Published in: ACS medicinal chemistry letters (2023)
Mitochondrial dysfunction has been attributed to many disease indications, including metabolic, cardiovascular, neoplastic, and neurodegenerative diseases. Dynamin related protein 1 (DRP1) is crucial in regulating mitochondrial fission and maintaining mitochondrial homeostasis. MiD49 is a dynamic peripheral protein receptor on the surface of the mitochondrial membrane that recruits DRP1 protein to induce mitochondrial binary fission. By targeting the protein-protein interaction of DRP1/MiD49, we have discovered a novel and potent allosteric DRP1 inhibitor that inhibits mitochondria fragmentation in vitro . X-ray cocrystal structure revealed that it locked the closed DRP1 conformation by induced dimerization.
Keyphrases
  • protein protein
  • small molecule
  • oxidative stress
  • cell death
  • magnetic resonance
  • single cell
  • computed tomography
  • mass spectrometry
  • reactive oxygen species
  • binding protein
  • drug induced